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- eset here or pull up for additional resources LO Provide the correct IUPAC name for the compound shown here. Question 18 of 18 ||วน d T Submit ON X-vise a Synthesis for the following conversion. Br Br6:00 PM Thu Apr 20 ●●●● Tap here or pull up for additional resources Question 15 of 16 Provide the correct IUPAC name for the compound shown here. 32% O Submit
- Predict the product(s) of the acid/base reactions below. Draw curved arrows to show the formation and breaking of bonds.16. Draw significant resonance structures for the following compound. Which of this is/are most significant resonance structure(s)? Explain why. (a) مهم (b) the H H- (c)Below is a structural formula. What is the corresponding condensed structural H formula? H1C1I Н Н OCH3NHC(CH3)2 H-CN-C-C CH3NHCH(CH3)2 OCH3NC(CH3)2 :Z―I OCH3NCH(CH3)2 H H H I— H -C-H H (
- Boc H3C Boc つい H₂C ·N ZI C H OH CH(CH3)CH₂CH3 H + DCC Na₂CO3, H₂O [(CH3)3COCO]20 C6H5CH₂OH, H† CH(CH3)CH₂CH3 H₂N CF3CO₂H H₂, Pd-C OH, H2O HBr, CH3COOH draw structure ... H |||| OCH₂C6H5 OCH₂C6H5Carboxylic Acid derivatives: Reaction of benzene-1,2-diol and carbonyl dichloride Part A Give the product formed when the following substances react together: Interactive 3D display mode *** OH 7 H 2D EXP. CONT OH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. 7 of 38 H3. Use curve-arrow notation to show electron flow in each of the following reactions and draw the structure of the product formed in each instance. a) HO 10: h) 10: cate :0: :0: :OH علق OH :0: HIC CH :OCH, O.. OH ww OH BOH NH, + Nall + HCO, + :NH₂
- 4. The scheme below shows the reaction of a ketone, 2-propanone with methanol. ОН :0 : || CH;-C-CH3 : ОН + H - Н CH,-C-CH3 CH;-C-CH3 N step 1 step 2 step 3 P CH;OH CH3 CH;OH step 4 OCH, CH,-C-CH3 H - H,0 R CH;-C-CH3 step 7 step 6 step 5 OCH3 OCH; i) Write the missing structures (N, O, Q and R) in the above reaction scheme. ii) Name the class of compounds P and S belong to? iii) This is an acid catalyzed reaction. What does this statement mean? iv) Draw the arrow diagram in step 6 to show how intermediate R is formed? Write the equation for this step ONLY. v) Steps 3 and 7 involve loss of a proton from the intermediate ions. Why is this step necessary?The molecule below is a metabolic precursor of both testosterone and estrone. What functional group(s) are present? A) Ketone CH3 B) Aldehyde CH3 H. C) Ether D) Ester E) Ether and ester 0日 PType here to search DELL でu ||||IPronto ((( ► 11 F8 Draw the major organic product formed when the compound shown below undergoes reaction with two equivalents of CH3CH₂CH₂Br, followed by aqueous workup. Interactive 3D display mode Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. EV X 5 F9 || C F10 NH₂ ? F11 F12 NO M 2